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dc.contributor.authorCarral Menoyo, Asier
dc.contributor.authorSotomayor Anduiza, María Nuria
dc.contributor.authorLete Expósito, María Esther
dc.date.accessioned2024-01-22T13:32:09Z
dc.date.available2024-01-22T13:32:09Z
dc.date.issued2020-09-15
dc.identifier.citationACS Omega 5 : 24974−24993 (2020)es_ES
dc.identifier.issn2470-1343
dc.identifier.urihttp://hdl.handle.net/10810/64179
dc.description.abstractThe use of earth-abundant first-row transition metals, such as cobalt, in C−H activation reactions for the construction and functionalization of a wide variety of structures has become a central topic in synthetic chemistry over the last few years. In this context, the emergence of cobalt catalysts bearing pentamethylcyclopentadienyl ligands (Cp*) has had a major impact on the development of synthetic methodologies. Cp*Co- (III) complexes have been proven to possess unique reactivity compared, for example, to their Rh(III) counterparts, obtaining improved chemo- or regioselectivities, as well as yielding new reactivities. This perspective is focused on recent advances on the alkylation and alkenylation reactions of (hetero)arenes with alkenes and alkynes under Cp*Co(III) catalysis.es_ES
dc.description.sponsorshipMinisterio de Ciencia e Innovación (PID2019-104148GB-I00), Gobierno Vasco (IT1045-16)es_ES
dc.language.isoenges_ES
dc.publisherACSes_ES
dc.relationinfo:eu-repo/grantAgreement/MICINN/PID2019-104148GB-I00es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es/*
dc.subjectcobaltes_ES
dc.subjectC-H activationes_ES
dc.subjecthydroarylationes_ES
dc.subjectalkenees_ES
dc.subjectalkynees_ES
dc.subjectmetal catalysises_ES
dc.titleCp*Co(III)-Catalyzed C−H Hydroarylation of Alkynes and Alkenes and Beyond: A Versatile Synthetic Tooles_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2020 American Chemical Society. This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.es_ES
dc.relation.publisherversionhttps://doi.org/10.1021/acsomega.0c03639es_ES
dc.identifier.doi10.1021/acsomega.0c03639
dc.departamentoesQuímica orgánica IIes_ES
dc.departamentoeuKimika organikoa IIes_ES


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© 2020 American Chemical Society. This is an open access article published under an ACS AuthorChoice License, which permits
copying and redistribution of the article or any adaptations for non-commercial purposes.
Except where otherwise noted, this item's license is described as © 2020 American Chemical Society. This is an open access article published under an ACS AuthorChoice License, which permits copying and redistribution of the article or any adaptations for non-commercial purposes.